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Expression of the Thyroid-Stimulating Hormone Receptor in the Folliculo-Stellate Cells of the Human Anterior Pituitary
TSH secretion from the anterior pituitary is mainly regulated by TRH and thyroid hormones. We hypothesized that in addition the pituitary itself could modulate TSH production by sensing its own TSH release, enabling fine-tuning of TSH secretion. For such an ultra-short loop control, the pituitary sh...
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Published in: | The journal of clinical endocrinology and metabolism 2000-11, Vol.85 (11), p.4347-4353 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | TSH secretion from the anterior pituitary is mainly regulated by TRH
and thyroid hormones. We hypothesized that in addition the pituitary
itself could modulate TSH production by sensing its own TSH release,
enabling fine-tuning of TSH secretion. For such an ultra-short loop
control, the pituitary should contain a TSH receptor (TSH-R). To find
evidence for this we screened a human pituitary complementary DNA
library with a digoxigenin-labeled TSH-R probe and found 2 positive
clones of 32,000 plaques. One clone was sequenced and found to be
completely identical to the thyroid TSH-R. Further proof was obtained
by RT-PCR on a human anterior pituitary obtained at autopsy. In
situ hybridization and immunohistochemistry confirmed the
presence of TSH-R in the anterior pituitary at the messenger
ribonucleic acid level as well as the protein level. Moreover, double
labeling experiments revealed that TSH-R messenger ribonucleic acid as
well as TSH-R protein colocalize with major histocompatibility complex
class II expression of folliculo-stellate cells. We conclude that TSH-R
is expressed in a subpopulation of folliculo-stellate cells in the
human anterior pituitary. This finding suggests ultra-short loop
regulation of TSH secretion. Putative recognition of the pituitary
TSH-R by TSH-R antibodies might have clinical relevance in Graves’
disease. |
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ISSN: | 0021-972X 1945-7197 |
DOI: | 10.1210/jcem.85.11.6991 |